共 33 条
- [1] Prenatal diagnosis of familial 3p26.3p25.3 deletion in a pregnancy associated with a favorable fetal outcome and asymptomatic carrier parent and family members in three generations JOURNAL OF STROKE & CEREBROVASCULAR DISEASES, 2024, 33 (09): : 561 - 564
- [2] Prenatal diagnosis of familial 2q13 microduplication and a de novo Xp22.33 microdeletion in a pregnancy associated with an asymptomatic mother carrier TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (01): : 174 - 177
- [3] Prenatal diagnosis of a familial 736-kb Xp22.2p22.13 microduplication encompassing NHS associated with an asymptomatic father carrier and no abnormality in the fetus TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (02): : 379 - 380
- [4] Prenatal diagnosis of a de novo 17p13.1 microduplication in a fetus with ventriculomegaly and lissencephaly TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2011, 50 (04): : 554 - 557
- [5] Prenatal diagnosis of familial 17q11.2 duplication encompassing NF1 in a pregnancy associated with asymptomatic carrier parent TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (03): : 426 - 427
- [6] Prenatal diagnosis of familial 266-kb 2q13 microquadruplication encompassing MALL and NPHP1 in a pregnancy associated with asymptomatic carrier parent TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2024, 63 (03): : 424 - 425
- [7] Prenatal diagnosis of a familial 9p12 amplification inherited from a father carrier TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2021, 60 (05): : 905 - 906
- [8] Prenatal diagnosis of a familial 21q22.3 microduplication encompassing part of Down syndrome critical region in a pregnancy associated with an asymptomatic mother carrier without Down syndrome phenotype TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2025, 64 (02): : 383 - 384
- [9] Prenatal diagnosis of familial transmission of 17q12 microduplication associated with no apparent phenotypic abnormality TAIWANESE JOURNAL OF OBSTETRICS & GYNECOLOGY, 2016, 55 (06): : 871 - 873